Biophysical and Biochemical Characterization of Lymphocytic Choriomeningitis Virus

Author:

Camyre Kenneth P.1,Pfau Charles J.1

Affiliation:

1. Department of Microbiology, University of Massachusetts, Amherst, Massachusetts 01002

Abstract

Biological, biochemical, and biophysical properties of three lymphocytic choriomeningitis (LCM) virus strains were compared. The biological property examined was the concentration range of virus which would, when injected into neonates, cause a carrier state. The dosage range for the CA1371 and Traub strains was found to be as broad as the limits examined (5 to 100 ld 50 units/mouse). The WCP strain, however, would only produce carriers within a 3 to 5 ld 50 range. The biochemical properties examined were the growth rates in tissue culture and the effect of varying the input ratio of virus to cells. With identical input ratios, the Traub strain reached a peak titer 32 hr after infection. The CA1371 and WCP strain reached their peaks at the 40th hr. With a 10-fold decrease in the amount of CA1371 virus per cell, peak titer (as high as in the above experiments) was not obtained until 56 hr postinfection. The biophysical properties examined were stability in density gradients and inactivation rates at 4C. In potassium tartrate gradients, full recovery of the CA1371 and WCP strain could be achieved. However, inactivation kinetics showed that only the CA1371 strain was much more stable than the Traub-LCM. The realization that marked differences in LCM strains exist is discussed in relation to certain inconsistencies in the literature.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference13 articles.

1. Demonstration of Iymphocytic choriomeningitis virus in cell cultures and mouse brain by the fluorescent antibody technique;BENDA R., V.;Acta Virol.,1965

2. Lymphocytic choriomeningitis in the mouse. II. Establishment of carrier colonies;LEHMANN-GR BE, F;Arch. Ges. Virusforsch.,1964

3. A carrier state of lymphocytic choriomeningitis virus in L cell cultures;LEHMANN-GR BE, F;Nature,1967

4. Immunofluorescence study of the carrier state and mechanism of vertical transmission in Iymphocytic choriomeningitis virus infection in mice;A.;J. Pathol. Bacteriol.,1966

5. Multiplication of Iymphocytic choriomeningitis virus in suspension cultures of Earle's strain L cells;PEDERSEN I. R.;Acta Pathol. Microbiol. Scand.,1966

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